Jestĕ k optimálnímu slození perorálního steroidního kontraceptiva
[Optimal composition of the peroral steroid contraceptive agent]

. 1977 May ; 42 (4) : 284-5.

Jazyk čeština Země Česko Médium print

Typ dokumentu anglický abstrakt, časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid00862059
Odkazy

PubMed 862059

The effects of exogenous estrogens on the liver are considered to be 1 of the more difficult obstacles in working out an optimal steroid contraceptive, as the liver is 1 of the specific terminal organs for estrogens. The estrogens used in oral steroid contraceptives are ethinyl estradiol (EE) and mestranol (ME). Attempts to overcome the effects of these exogenous estrogens has lead to investigations of the possibilities of gestagens, which have a significant effect on cytoplasmatic receptors in the cells of the terminal tissues. An optimal steroid compound, which maximizes the contraceptive action while minimizing the side effects has been worked out, consisting of daily doses of .03 mg of EE and .15 mg of d-norgestrel. This compound is considered to sufficiently compensate the estrogen effects of its estrogen component through the action of the gestagen component.

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